Bruce Gelb

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Bruce Gelb

MD

 https://orcid.org/0000-0001-8527-5027
Calculated based on number of publications stored in Pure and citations from Scopus
1989 …2023

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  • 2016

    Genetic discovery for congenital heart defects

    Gelb, B. D., 1 Jan 2016, Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology. Springer Japan, p. 355-360 6 p.

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

    Open Access
    3 Scopus citations
  • 2013

    Molecular genetics of congenital heart disease

    Carey, A. S. & Gelb, B. D., 1 Mar 2013, Molecular Genetic Pathology: Second Edition. Springer New York, Vol. 9781461448006. p. 591-605 15 p.

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

  • 2012

    Genetics of Congenital Heart Disease

    Gelb, B. D. & Chin, S. E., 18 Jul 2012, Muscle: Fundamental Biology and Mechanisms of Disease. Elsevier, Vol. 1-2. p. 473-480 8 p.

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

    3 Scopus citations

  • Genetic Testing

    Madan, N. & Gelb, B. D., 13 Jan 2012, Pediatric Cardiovascular Medicine: Second Edition. Wiley-Blackwell, p. 222-230 9 p.

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

  • 2009

    LEOPARD syndrome: Clinical aspects and molecular pathogenesis

    Sarkozy, A., Digilio, M. C., Zampino, G., Dallapiccola, B., Tartaglia, M. & Gelb, B. D., 2009, Noonan Syndrome and Related Disorders - A Matter of Deregulated Ras Signaling. Zenker, M. (ed.). p. 55-65 11 p. (Monographs in Human Genetics; vol. 17).

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

    12 Scopus citations

  • Molecular genetics of Noonan syndrome

    Tartaglia, M. & Gelb, B. D., 2009, Noonan Syndrome and Related Disorders - A Matter of Deregulated Ras Signaling. Zenker, M. (ed.). p. 20-39 20 p. (Monographs in Human Genetics; vol. 17).

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

    9 Scopus citations
  • 2007

    Char Syndrome and TFAP2B Mutations

    Gelb, B. D., 16 Nov 2007, Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. Blackwell Publishing Ltd., p. 253-259 7 p.

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

  • Noonan Syndrome and PTPN11 Mutations

    Tartaglia, M. & Gelb, B. D., 16 Nov 2007, Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. Blackwell Publishing Ltd., p. 263-272 10 p.

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review